A precise 90/spl deg/ quadrature OTA-C oscillator tunable in the 50-130-MHz range

We present a very-large-scale integration continuous-time sinusoidal operational transconductance amplifiers quadrature oscillator fabricated in a standard double-poly 0.8-/spl mu/m CMOS process. The oscillator is tunable in the frequency range from 50 to 130 MHz. The two phases produced by the oscillator show a low-quadrature phase error. A novel current-mode amplitude control scheme is developed that allows for very small amplitudes. Stability of the amplitude control loop is studied as well as design considerations for its optimization. Experimental results are provided.     

Influence of the 4,6-O-benzylidene, 4,6-O-phenylboronate, and 4,6-O-polystyrylboronate protecting groups on the stereochemical outcome of thioglycoside-based glycosylations mediated by 1-benzenesulfinyl piperidine/triflic anhydride and N-iodosuccinimide/trimethylsilyl triflate

The effect of 4,6-O-benzylidene acetals, 4,6-O-phenylboronate esters, and 4,6-O-polystyrylboronate esters on the stereoselectivity of couplings to galacto-, gluco-, and mannopyranosyl thioglycosides, otherwise protected with benzyl ethers, has been investigated by the benzenesulfinyl piperidine/trifluoromethanesulfonic anhydride (BSP), diphenyl sulfoxide/trifluoromethanesulfonic anhydride (Ph(2)SO), and N-iodosuccinimide/trimethylsilyl trifluoromethanesulfonate (NIS/TMSOTf) methods. The BSP and Ph(2)SO methods give comparable results in all three systems whereas the NIS method affords significantly different stereoselectivities in both the gluco and manno, but not the galacto series. The benzylidene acetal and boronate esters influence the stereochemistry in a similar manner in the beta-selective manno series and the alpha-selective galacto series but show significant differences with the glucose donors. The differences between the glucose, galactose, and mannose series reflect the established differences in reactivity and, especially for mannose, those in the anomeric effect and are best interpreted in terms of changes in the relative energetics between the alpha- and beta-covalent triflate intermediates and the various contact ion pairs with which they are necessarily in equilibrium.     

Compositional, structural, optical and electrical characterization of CulnTe2 grown by the tellurization of stoichiometric Cu and in in the liquid phase

A new method to grow single crystals with stoichiometry close to 1:1:2 of CuInTe₂, an important member of the Cu-III-VI₂ family of semiconductors is described. This consists of tellurization in the liquid phase of stoichiometric Cu and In and later solidification under directional freezing. It is found from energy dispersive spectroscopy that the ingots obtained with the evaporation temperature (T_t) of Te at 590 and 635°C were very close to the ideal stoichiometry 1:1:2. Samples of all ingots obtained with T_t between 530 and 690°C, as studied by x-ray and differential thermal analysis, were of single phase having chalcopyrite structure and p-type conductivity. Optical and electrical characterization of different ingots were made. The acceptor ionization energy E_A and the density of states effective mass m _p ^* of the holes are estimated from the temperature dependence of the hole concentration p in samples of different ingots. m _p ^* = (0.78 ± 0.02) m_e agrees quite well with the reported value. From a combined analysis of the variation of E_A with p^1/3 and the knowledge of molecularity and valence stoichiometry of each sample, it is established that the shallow acceptor level observed in different samples with E_A (0) ⋍ 30 meV is due to V_In.     

Transitions to the Fulde-Ferrell-Larkin-Ovchinnikov phases at low temperature in two dimensions

We explore the nature of the transition to the Fulde-Ferrell-Larkin- Ovchinnikov superfluid phases in the low temperature range in two dimensions, for the simplest isotropic BCS model. This is done by applying the Larkin-Ovchinnikov approach to this second order transition. We show that there is a succession of transitions toward ever more complex order parameters when the temperature goes to zero. This gives rise to a cascade with, in principle, an infinite number of transitions. Except for one case, the order parameter at the transition is a real superposition of cosines with equal weights. The directions of these wavevectors are equally spaced angularly, with a spacing which goes to zero when the temperature goes to zero. This singular behaviour in this T = 0 limit is deeply linked to the two-dimensional nature of the problem.     

Diamond electrode facilitated electrosynthesis of water and wastewater treatment oxidants

While diamond electrodes have been commonly used to generate ^?OH to treat a variety of persistent water and wastewater micropollutants, mass transfer limitations and the non-selective, short-lived nature of the ^?OH restrict the degradation to the solution at, or near, the electrode surface. However, diamond electrodes can generate oxidizing species that facilitate micropollutant degradation in the bulk water solution. These include persulfate, sulfate radicals, peroxodiphosphate, ferrate, permanganate, reactive chlorine species, hydrogen peroxide, and ozone, which have been reported during electrochemical treatment of water with diamond electrodes. Although still restricted to specialized applications, recent studies, summarized in this review, have proven the electrogeneration of these additional oxidant species to be effective. They have shown the adaptability and potential of diamond electrode-based water treatment to mitigate the presence of micropollutants in water.     

The kinetics of the attachment of polymer chains to reactive latex particles and the resulting latex stabilization

Poly(vinyl benzyl chloride) latex was reacted with ethanolamine and with amine terminated chain molecules containing up to 33 ethylene oxide residues. The kinetics of these reactions were essentially independent of the length of the chain carrying the amine group. An increasing length of the chains bound to the surface of the latex particles produced an increasing latex stabilization.     

Capillary electrophoresis method for analysis of inorganic and organic anions related to habitability and the search for life

In situ missions of exploration require analytical methods that are capable of detecting a wide range of molecular targets in complex matrices without a priori assumptions of sample composition. Furthermore, these methods should minimize the number of reagents needed and any sample preparation steps. We have developed a method for the detection of metabolically relevant inorganic and organic anions that is suitable for implementation on in situ spaceflight missions. Using 55 mM acetic acid, 50 mM triethylamine, and 5% glycerol, more than 21 relevant anions are separated in less than 20 min. The method is robust to sample ionic strength, tolerating high concentrations of background salts (up to 900 mM NaCl and 300 mM MgSO₄). This is an important feature for future missions to ocean worlds. The method was validated using a culture of Escherichia coli and with high salinity natural samples collected from Mono Lake, California.